TBC1D7 Chromosome 6

TBC1 domain family member 7
11 variants 11 Health Risk

Upload your DNA to see your personal genotypes for variants in TBC1D7.

What This Gene Does
This gene encodes a member of the TBC-domain containing protein family. The encoded protein functions as a subunit of the tuberous sclerosis TSC1-TSC2 complex which plays a role in the regulation of cellular growth and differentiation. Mutations in this gene have been associated with autosomal recessive megalencephaly. Alternative splicing results in multiple transcript variants. Naturally occurring readthrough transcription occurs between this locus and downstream LOC100130357. [provided by RefSeq, Jan 2016]
Gene Info
Gene Group
TSC complex
Locus Type
gene with protein product
Location
6p24.1
Ensembl
ENSG00000145979
Associated Conditions (3)
Macrocephaly
Macrocephaly/megalencephaly syndrome
autosomal recessive
Key Variants
All Variants (11)
RSID Category Clinical Significance Conditions
RS112668572 Health Risk Conflicting classifications of pathogenicity
RS150455776 Health Risk Conflicting classifications of pathogenicity
RS151071014 Health Risk Conflicting classifications of pathogenicity
RS1554192525 Health Risk Conflicting classifications of pathogenicity Macrocephaly, Macrocephaly
RS549062038 Health Risk Conflicting classifications of pathogenicity
RS1584522453 Health Risk Likely pathogenic
RS2480565963 Health Risk Likely pathogenic
RS1324026596 Health Risk Pathogenic
RS483352922 Health Risk Pathogenic Macrocephaly/megalencephaly syndrome, autosomal recessive, Macrocephaly/megalencephaly syndrome
RS587777652 Health Risk Pathogenic Macrocephaly/megalencephaly syndrome, autosomal recessive, Macrocephaly/megalencephaly syndrome
RS758759342 Health Risk Pathogenic Macrocephaly/megalencephaly syndrome, autosomal recessive, Macrocephaly/megalencephaly syndrome
Sign Up to Analyze Your DNA Log In